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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2011 | 1 |
2019 | 1 |
2022 | 1 |
2024 | 0 |
PubMed (GeneRIF) for id: 212919
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Kctd7 deficiency induces myoclonic seizures associated with Purkinje cell death and microvascular defects.
Dis Model Mech. 2022 Sep 1;15(9):dmm049642. doi: 10.1242/dmm.049642. Epub 2022 Sep 13.
Dis Model Mech. 2022.
PMID: 35972048
Free PMC article.
Progressive myoclonic epilepsy-associated gene Kctd7 regulates retinal neurovascular patterning and function.
Alevy J, Burger CA, Albrecht NE, Jiang D, Samuel MA.
Alevy J, et al.
Neurochem Int. 2019 Oct;129:104486. doi: 10.1016/j.neuint.2019.104486. Epub 2019 Jun 6.
Neurochem Int. 2019.
PMID: 31175897
Free PMC article.
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Progressive myoclonic epilepsy-associated gene KCTD7 is a regulator of potassium conductance in neurons.
Azizieh R, Orduz D, Van Bogaert P, Bouschet T, Rodriguez W, Schiffmann SN, Pirson I, Abramowicz MJ.
Azizieh R, et al.
Mol Neurobiol. 2011 Aug;44(1):111-21. doi: 10.1007/s12035-011-8194-0. Epub 2011 Jun 28.
Mol Neurobiol. 2011.
PMID: 21710140
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